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Published on: March 10, 2021
The Moraxella catarrhalis immunoglobulin D-binding protein MID has conserved sequences and is regulated by a
Andrea Möllenkvist1, Therése Nordström, Christer Halldén
1Department of Medical Microbiology, Malmö University Hospital, Lund University, SE-205 02 Malmö, Sweden.
Abstract:
The prevalence of the Moraxella catarrhalis immunoglobulin D (IgD)-binding outer membrane protein MID and its gene was determined in 91 clinical isolates and in 7 culture collection strains. Eighty-four percent of the clinical Moraxella strains expressed MID-dependent IgD binding. The mid gene was detected in all strains as revealed by homology of the signal peptide sequence and a conserved area in the 3' end of the gene. When MID proteins from five different strains were compared, an identity of 65.3 to 85.0% and a similarity of 71.2 to 89.1% were detected. Gene analyses showed several amino acid repeat motifs in the open reading frames, and MID could be called a putative autotransport protein. Interestingly, homopolymeric [polyguanine [poly(G)]] tracts were detected at the 5' ends within the open reading frames. By flow cytometry, using human IgD and fluorescein isothiocyanate-conjugated anti-IgD polyclonal antibodies, most strains showed two peaks: one high- and one low-intensity peak. All isolates expressing high levels of MID had 1, 2, or 3 triplets of G's in their poly(G) tracts, while strains not expressing MID had 4, 7, 8, or 10 G's in their poly(G) tracts or point mutations causing a putative preterminated translation. Northern blot analysis revealed that the mid gene was regulated at the transcriptional level. Experiments with nonclumping variants of M. catarrhalis proved that bacteria lost their MID expression by removing a G in their poly(G) tracts. Moraxella strains isolated from the nasopharynx or from blood and sputum specimens expressed MID at approximately the same frequency. In addition, no variation was observed between strains of different geographical origins (Australia, Europe, Japan, or the United States). MID and the mid gene were found solely in M. catarrhalis, whereas related Neisseria and Moraxella species did not express MID. Taken together, MID appears to be a conserved protein that can be found in essentially all M. catarrhalis strains. Furthermore, MID is governed by poly(G) tracts when bacteria undergo phase variation.
Insights
Moraxella catarrhalis immunoglobulin D (IgD)-binding outer membrane protein MID is present in nearly all strains. Its expression is controlled by polyguanine tracts, influencing bacterial phase variation.
Area of Science:
- Microbiology
- Molecular Biology
- Immunology
Background:
- Moraxella catarrhalis is a significant human pathogen.
- Immunoglobulin D (IgD) binding proteins on bacterial surfaces can influence host-pathogen interactions.
- The outer membrane protein MID and its role in IgD binding were not fully characterized.
Purpose of the Study:
- To determine the prevalence of the MID protein and its gene in Moraxella catarrhalis.
- To investigate the genetic basis and regulation of MID expression.
- To explore the potential role of MID in bacterial phase variation.
Main Methods:
- Prevalence study on clinical and culture collection isolates.
- Gene sequencing and homology analysis.
- Flow cytometry for protein expression analysis.
- Northern blot for transcriptional regulation.
- Mutational analysis of polyguanine tracts.
Main Results:
- 84% of clinical Moraxella strains expressed MID-dependent IgD binding.
- The mid gene was detected in all strains, showing 65.3-85.0% identity between different strains.
- MID expression levels correlated with the number of G's in poly(G) tracts at the 5' end of the open reading frame.
- MID expression is regulated at the transcriptional level and influenced by poly(G) tract length, mediating phase variation.
Conclusions:
- MID is a conserved protein found in almost all Moraxella catarrhalis strains.
- Polyguanine tracts within the mid gene regulate MID expression through phase variation.
- MID appears to be a unique marker for Moraxella catarrhalis, not found in related species.
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